Introduction

A description of the various stages and sections of a Master Regulatory File (MRF) System. As an investigational product progresses through development key studies, decisions, regulatory communications, manufacturing progression are accumulated and necessary to reference as the NDA and MAA applications are made. Therefore MRF systems needs to preplanned and have sections to organize this information. Although this won't be discussed this organization is applicable to a well managed document management system.

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online

online, 201,N Squirrel road,, Auburn Hills, Suite 1007, michigan, 48326, United States

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Organised by

Global Compliance Trainings

Contact information

Mr john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, michigan, 48326, United States of America
2482120588
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